JPH04114744A - Deodorizing catalyst and heating apparatus using the same - Google Patents
Deodorizing catalyst and heating apparatus using the sameInfo
- Publication number
- JPH04114744A JPH04114744A JP2232722A JP23272290A JPH04114744A JP H04114744 A JPH04114744 A JP H04114744A JP 2232722 A JP2232722 A JP 2232722A JP 23272290 A JP23272290 A JP 23272290A JP H04114744 A JPH04114744 A JP H04114744A
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- deodorizing
- deodorizing catalyst
- porous material
- honeycomb
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 49
- 230000001877 deodorizing effect Effects 0.000 title claims abstract description 31
- 238000010438 heat treatment Methods 0.000 title claims abstract description 10
- 239000011148 porous material Substances 0.000 claims abstract description 60
- 235000013305 food Nutrition 0.000 claims abstract description 13
- 239000011572 manganese Substances 0.000 claims abstract description 12
- 229910052878 cordierite Inorganic materials 0.000 claims abstract description 9
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 9
- 229910052709 silver Inorganic materials 0.000 claims abstract description 9
- 239000000779 smoke Substances 0.000 claims abstract description 9
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000004332 silver Substances 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 6
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052863 mullite Inorganic materials 0.000 claims abstract description 5
- 238000010422 painting Methods 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 5
- 239000011248 coating agent Substances 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 abstract description 2
- 239000000428 dust Substances 0.000 abstract 1
- 241000264877 Hippospongia communis Species 0.000 description 37
- 230000000052 comparative effect Effects 0.000 description 23
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 12
- 238000010411 cooking Methods 0.000 description 6
- 238000010586 diagram Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
Landscapes
- Catalysts (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は調理器、ゴミ焼却炉、塗装装置等の加熱袋!お
よびその脱臭触媒に係わり、特に処理中の食品、ゴミ等
から発生する可燃性の有機臭気成分の低減・除去に好適
な脱臭触媒に関する。[Detailed Description of the Invention] [Industrial Field of Application] The present invention is a heating bag for cooking appliances, garbage incinerators, painting equipment, etc.! The present invention relates to a deodorizing catalyst thereof, and particularly to a deodorizing catalyst suitable for reducing and removing flammable organic odor components generated from food products, garbage, etc. during processing.
[従来の技術]
オーブンやコンロ等の食品調理器の使用上の問題の一つ
は、調理器内で加熱された食品もしくは食品飛散物から
発生する煙や排ガス中に含まれる悪臭成分が家屋内に広
がり家具、壁、カーペット等に吸着され比較的長時間に
渡って悪臭を放つことである。この対策として最近の食
品調理器では発生した煙や排ガスを吸引し、触媒に接触
させて悪臭成分を酸化し、除去 低減する装置を取り付
けたものが多い。[Prior Art] One of the problems with using food cooking appliances such as ovens and stoves is that malodorous components contained in smoke and exhaust gas generated from food heated in the cooking appliance or from food particles can enter the house. It spreads and is adsorbed to furniture, walls, carpets, etc., emitting a bad odor for a relatively long period of time. As a countermeasure to this problem, many modern food cookers are equipped with devices that suck the generated smoke and exhaust gas, bring it into contact with a catalyst, and oxidize the malodorous components to eliminate and reduce the amount of malodorous components.
前記食品調理装置に限らずゴミ焼却炉、塗装装置等の加
熱装置の悪臭低減、除去用に使用される触媒として銀(
Ag)とマンガン(Mn)を組合わせた触媒は優れた低
温活性を示すことが知られている(田部浩三、清山哲部
、笛木和雄編、「金属酸化物と複合酸化物、 197
8.4.20講談社サイエンティフィク、16頁)、こ
の種の触媒は通常、比表面積は数m2/g以下の高強度
で耐熱性のある基材に予め活性アルミナのような高比表
面積担体をウォッシュコートして、その後触媒成分を食
潰法等により担持させて調製される。Silver (
It is known that a catalyst combining Ag) and manganese (Mn) exhibits excellent low-temperature activity (Kozo Tabe, Tetsube Kiyoyama, Kazuo Fueki, eds., Metal Oxides and Composite Oxides, 197
8.4.20 Kodansha Scientific, p. 16), this type of catalyst is usually coated with a high specific surface area support such as activated alumina on a high strength and heat resistant base material with a specific surface area of several m2/g or less. It is prepared by wash-coating and then supporting the catalyst component by a crushing method or the like.
[発明が解決しようとする課M]
しかし、前記調製法によって得られるAgとMnを組合
わせた触媒は使用条件によっては、つオツシュコート層
がはく離することがあった。特に、食品調理用オーブン
等に使用するときには、はく離した前記触媒が食品に降
りかかることは大きな問題であった。[Problem M to be Solved by the Invention] However, depending on the conditions of use, the catalyst layer obtained by combining Ag and Mn obtained by the above-mentioned preparation method may peel off. Particularly when used in food cooking ovens, etc., it has been a big problem that the peeled off catalyst falls on the food.
また、前記A g / M n系触媒は一般に300℃
近くの温度で、その機能を発現するので、通常は触媒も
しくは処理する煙や排ガスを予熱する機構を持っている
。しかし、この予熱のために、食品調理装置の場合、そ
の消費電力の30%から40%を煙や排ガスを予熱する
ために消費する。さらに、予熱機構とその周囲の断熱の
ため、装置内の多くの容積を取るので装置の小型、軽量
化の障害の一つとなっている。In addition, the A g / M n type catalyst is generally heated at 300°C.
Since it performs its function at a nearby temperature, it usually has a catalyst or a mechanism to preheat the smoke or exhaust gas to be treated. However, due to this preheating, in the case of a food cooking device, 30% to 40% of its power consumption is consumed for preheating smoke and exhaust gas. Furthermore, the preheating mechanism and its surrounding insulation require a large volume inside the device, which is one of the obstacles to making the device smaller and lighter.
そこで、本発明の目的は耐はく離性とAg/Mn系脱臭
触媒の低温活性を向上させ、脱臭触媒の予熱機構を軽減
もしくは省略することにある。Therefore, an object of the present invention is to improve the peeling resistance and low-temperature activity of an Ag/Mn-based deodorizing catalyst, and to reduce or omit the preheating mechanism of the deodorizing catalyst.
[課題を解決するための手段] 本発明の上記目的は次の構成により、達成される。[Means to solve the problem] The above object of the present invention is achieved by the following configuration.
すなわち、食品調理器、ゴミ焼却炉、塗装装置等の加熱
装置から発生する煙や排ガス中に含まれる臭気成分を低
減もしくは除去する脱臭触媒において、銀とマンガンの
元素またはその化合物を含む活性成分を、全細孔容積が
0 、20 c m3/′g以上で半径1,000人か
ら30,000人の範囲の細孔の容積の合計量が全細孔
容積の80v。In other words, in deodorizing catalysts that reduce or remove odor components contained in smoke and exhaust gas generated from heating equipment such as food cookers, garbage incinerators, and painting equipment, active ingredients containing silver and manganese elements or their compounds are used. , the total pore volume is 0, 20 cm3/'g or more, and the total volume of pores in the radius range from 1,000 to 30,000 is 80V of the total pore volume.
1%以上である細孔分布を有するコーディエライト、ム
ライト、アルミナ等からなる多孔質材料に担持する脱臭
用触媒、または、
前記脱臭用触媒を排気部に配置した加熱装置、である。A deodorizing catalyst supported on a porous material such as cordierite, mullite, alumina, etc. having a pore distribution of 1% or more, or a heating device in which the deodorizing catalyst is disposed in an exhaust section.
[作用]
本発明の脱臭用触媒はウォッシュコートを用いないで、
直接前記全細孔容積と細孔分布を有するコーディエライ
ト、ムライト、アルミナ等からなる多孔質材料に担持す
るので、触媒が多孔質材料からはく離することがない。[Function] The deodorizing catalyst of the present invention does not use a wash coat,
Since the catalyst is directly supported on a porous material made of cordierite, mullite, alumina, etc. having the above-mentioned total pore volume and pore distribution, the catalyst does not peel off from the porous material.
また、前記脱臭用触媒は比較的低温で脱臭活性があり、
食品調理器、ゴミ焼却炉、塗装装置等の加熱装置から発
生する煙や排ガス中に含まれる臭気成分を低減もしくは
除去することができる。Further, the deodorizing catalyst has deodorizing activity at a relatively low temperature,
Odor components contained in smoke and exhaust gas generated from heating devices such as food cookers, garbage incinerators, and painting equipment can be reduced or removed.
[実施例] 本発明の実施例および比較例を図面を用いて説明する。[Example] Examples and comparative examples of the present invention will be described with reference to the drawings.
なお、本実施例および比較例に用いる触媒担体としてコ
ーディエライトハニカムを使用したが、これに限らず、
ムライト、アルミナ等の多孔質材料も使用可能である。Although cordierite honeycomb was used as the catalyst carrier in the present examples and comparative examples, the present invention is not limited to this.
Porous materials such as mullite and alumina can also be used.
また、多孔質材料の形状はハニカム以外の粒状、球状、
板状等でもよい。また、本実施例ではハニカムの全細孔
容積および細孔分布は水銀ポロシメータで細孔半径が2
50μmから30人の範囲のものを測定した。In addition, the shape of the porous material may be granular, spherical, or
It may be plate-shaped or the like. In addition, in this example, the total pore volume and pore distribution of the honeycomb were measured using a mercury porosimeter with a pore radius of 2.
The measurements ranged from 50 μm to 30 people.
第1図に実施例および比較例の脱臭用触媒に使用したセ
ル密度が200セル/1nch2のコーディエライトハ
ニカム1の形状を示した。寸法は幅150mm、高さ4
0mm、セル方向の長さ20mmである。FIG. 1 shows the shape of a cordierite honeycomb 1 with a cell density of 200 cells/1 nch2 used in the deodorizing catalysts of Examples and Comparative Examples. Dimensions are width 150mm, height 4
0 mm, and the length in the cell direction is 20 mm.
実施例1
全細孔容積が0.37cc/gのハニカムAを硝MWI
と硝酸マンガンの50wt%の水溶液に含浸し、次に5
00℃で2時間焼成して、銀とマンガンの混合化合物を
40g/I担持した実施例1の脱臭触媒を調製した。Example 1 Honeycomb A with a total pore volume of 0.37 cc/g was treated with nitric MWI
and manganese nitrate in a 50 wt% aqueous solution, then 5
The deodorizing catalyst of Example 1 was prepared by calcining at 00° C. for 2 hours and carrying 40 g/I of a mixed compound of silver and manganese.
実施例2
ハニカムAを追加焼成し、全細孔容積0.20c c
/ gとしたハニカムBに実施例1と同様に銀とマンガ
ンの混合化合物を40g/l担持し、実施例2の脱臭触
媒とした。Example 2 Honeycomb A was additionally fired, and the total pore volume was 0.20 c c
Similarly to Example 1, 40 g/l of a mixed compound of silver and manganese was supported on Honeycomb B, which had a concentration of 40 g/g, to provide the deodorizing catalyst of Example 2.
比較例1
ハニカムBをさらに追加焼成し、全細孔容積を0.17
cc/gに減少させたハニカムCを実施例と同条件で触
媒調製したものを比較例1とした。Comparative Example 1 Honeycomb B was further fired to reduce the total pore volume to 0.17.
Comparative Example 1 was obtained by preparing a catalyst under the same conditions as in the example using honeycomb C reduced to cc/g.
第2図に実施例1、実施例2および比較例1に用いたハ
ニカムの細孔分布を示した。FIG. 2 shows the pore distribution of the honeycombs used in Example 1, Example 2, and Comparative Example 1.
各ハニカムは全細孔容積が異なるので細孔分布のピーク
の大きさは異なるが、半径が1.000人から30,0
00人の範囲の細孔を持つハニカムも多く、その範囲内
の細孔の容積の合計は各全細孔容積の80%以上を占め
る。Each honeycomb has a different total pore volume, so the peak size of the pore distribution is different, but the radius ranges from 1.000 to 30.0
There are many honeycombs having pores in the range of 0.00 to 0.00, and the total volume of pores within this range accounts for 80% or more of the total pore volume.
比較例2および比較例3
第3図にハニカムDとハニカムEの細孔分布を示す。ハ
ニカムDとハニカムEは細孔分布がハニカムBと異なる
ようにコーディエライト原料の粒径を調製し、焼成条件
をかえて全細孔容積をハニカムDは0.21cc/g、
ハニカムEは0.20 c c / gとハニカムBと
同程度に合わせたハニカムである。Comparative Example 2 and Comparative Example 3 Figure 3 shows the pore distribution of Honeycomb D and Honeycomb E. For Honeycomb D and Honeycomb E, the particle size of the cordierite raw material was adjusted so that the pore distribution was different from Honeycomb B, and the firing conditions were changed so that the total pore volume for Honeycomb D was 0.21 cc/g;
Honeycomb E is a honeycomb with a density of 0.20 c c / g, which is the same as honeycomb B.
ハニカムDは比較的粒径の細かい原料を使用したので、
細孔分布はハニカムBより半径の小さい細孔が多く、6
00人から5,000人の間に集中している。ハニカム
Eは逆に粒径の比較的粗い原料を使用したので、細孔は
半径がs、ooo人からso、ooo人の間に集中して
いる。Honeycomb D uses raw materials with relatively fine particle size, so
The pore distribution has more pores with a smaller radius than honeycomb B;
The population is concentrated between 00 and 5,000. On the contrary, honeycomb E used a raw material with a relatively coarse particle size, so the pores were concentrated between radii of s, ooo and so, ooo.
この両ハニカムを用いて実施例2と同条件となるように
銀とマンガンの混合化合物を担持して比較例2および比
較例3を調製した。Comparative Example 2 and Comparative Example 3 were prepared by using both honeycombs to support a mixed compound of silver and manganese under the same conditions as in Example 2.
以上調製したハニカムの特性を第1表に示す。Table 1 shows the characteristics of the honeycomb prepared above.
第1表
第4図にハニカムの全細孔容積が0.37cc/gの実
施例1.0.20cc/gの実施例2および0.17c
c/gの比較例1の脱臭性能の温度特性をそれぞれ示し
た。各触媒のハニカムは全細孔容積は異なるが、細孔分
布は類似しており半径が1,000人から30,000
人の細孔の容積が全細孔容積の80%以上を占める。Table 1 and Figure 4 show Example 1 in which the total pore volume of the honeycomb is 0.37cc/g, Example 2 in which the total pore volume of the honeycomb is 0.20cc/g, and 0.17c.
The temperature characteristics of the deodorizing performance of Comparative Example 1 of c/g are shown. Although the honeycombs of each catalyst differ in total pore volume, the pore distribution is similar and the radius ranges from 1,000 to 30,000.
The volume of human pores accounts for more than 80% of the total pore volume.
なお、脱臭用触媒の性能評価は臭気成分としてアセトア
ルデヒドを選び、これを1100pp含む空気を触媒に
30,0OOh−’の空気速度で接触させアセトアルデ
ヒドの除去率を測定した。In order to evaluate the performance of the deodorizing catalyst, acetaldehyde was selected as the odor component, air containing 1100 pp of acetaldehyde was brought into contact with the catalyst at an air velocity of 30.0 OOh-', and the removal rate of acetaldehyde was measured.
各触媒ともアセトアルデヒドを除去し始める触媒温度に
特に差は認められないが、完全除去するのに必、要な触
媒温度には差があり、仮に90%以上の除去率を得るの
に必要な触媒温度で比較すると実施例1と実施例2は1
80℃付近である。これに対し比較例1は220℃に達
しており、全細孔容積が触媒の性能に影響すること、ま
たその値が少なくとも0.20cc/g以上必要なこと
が明らかになった。There is no particular difference in the catalyst temperature at which acetaldehyde begins to be removed, but there is a difference in the catalyst temperature required to completely remove acetaldehyde. Comparing the temperature, Example 1 and Example 2 are 1
The temperature is around 80°C. On the other hand, in Comparative Example 1, the temperature reached 220°C, making it clear that the total pore volume affects the performance of the catalyst, and that the value needs to be at least 0.20 cc/g.
第5図に、脱臭用触媒の性能に及ぼすハニカムの細孔分
布の影響を調べるため、全細孔容積を80%以上占める
細孔の半径の範囲が600人がら5.000人の比較例
2、同じ<1,000人から30,000人の実施例2
および同じ<8,000人から80,000人の比較例
3の脱臭性能の温度特性を比較した。その結果、実施例
2のものが最も低い触媒温度で高いアセトアルデヒド除
去率が得られ、これにより径の小さな細孔が多い比較例
2のものと径の大きな細孔が多い比較例3のものはより
高い温度が必要であることがら、触媒に使用するハニカ
ムの細孔分布はハニカムAおよびハニカムBのようなも
のが適正であることが判明した。Figure 5 shows Comparative Example 2 in which the radius of pores that account for 80% or more of the total pore volume ranges from 600 to 5,000 people in order to investigate the influence of the pore distribution of the honeycomb on the performance of the deodorizing catalyst. , same<1,000 to 30,000 people Example 2
The temperature characteristics of the deodorizing performance of Comparative Example 3 were compared between <8,000 and 80,000 people. As a result, a high acetaldehyde removal rate was obtained in Example 2 at the lowest catalyst temperature, and as a result, Comparative Example 2, which had many small-diameter pores, and Comparative Example 3, which had many large-diameter pores, Since a higher temperature is required, it has been found that honeycombs such as Honeycomb A and Honeycomb B are suitable for the pore distribution of honeycombs used in the catalyst.
本実施例の脱臭用触媒は食品調理器に限らず、ゴミ焼却
炉、塗装装置等の加熱装置がら発生する煙や排ガス中に
含まれる臭気成分の低減もしくは除去にも使用される。The deodorizing catalyst of this embodiment is used not only for food cooking devices but also for reducing or removing odor components contained in smoke and exhaust gas generated from heating devices such as garbage incinerators and painting devices.
[発明の効果]
本発明によれば、脱臭用触媒の低温活性が向上するので
、脱臭用触媒を組込んだ装置の触媒予熱用の機構が省略
もしくは軽減できるので装置の小型・軽量化が図れ、ま
た、予熱機構に消費されるエネルギーを低減することが
できる。さらに、脱臭触媒の耐はく離性が高いので、触
媒担体がらはく離することがない。[Effects of the Invention] According to the present invention, since the low-temperature activity of the deodorizing catalyst is improved, the catalyst preheating mechanism of the device incorporating the deodorizing catalyst can be omitted or reduced, and the device can be made smaller and lighter. Moreover, the energy consumed by the preheating mechanism can be reduced. Furthermore, since the deodorizing catalyst has high peeling resistance, the catalyst carrier does not peel off.
第1図は本発明の実施例および比較例に用いた多孔質の
コーディエライトハニカムの外観図、第2図は本発明の
実施例1、実施例2および比較例1に用いたハニカムの
細孔分布を示した図、第3図は比較例2と比較例3に用
いたハニカムの細孔分布を示した図、第4図は本発明の
実施例1、実施例2および比較例1の脱臭特性の温度特
性を示した図、第5図は本発明の実施例2、比較例2お
よび比較例3の脱臭特性の温度特性を示した図である。
出願人 バブコック日立株式会社
代理人 弁理士 松永孝義 ほか1名
第
図
細孔半径(入)
第
図
触媒
温度(”C)
単位:mm
細孔半径(人)
度(°C)Figure 1 is an external view of a porous cordierite honeycomb used in Examples and Comparative Examples of the present invention, and Figure 2 is a detailed view of the honeycomb used in Example 1, Example 2, and Comparative Example 1 of the present invention. Figure 3 shows the pore distribution of the honeycombs used in Comparative Example 2 and Comparative Example 3. Figure 4 shows the pore distribution of the honeycombs used in Example 1, Example 2, and Comparative Example 1 of the present invention. FIG. 5 is a diagram showing the temperature characteristics of the deodorizing characteristics of Example 2, Comparative Example 2, and Comparative Example 3 of the present invention. Applicant Babcock-Hitachi Co., Ltd. Agent Patent attorney Takayoshi Matsunaga and one other person Diagram Pore radius (in) Diagram Catalyst temperature (''C) Unit: mm Pore radius (person) Degrees (°C)
Claims (2)
から発生する煙や排ガス中に含まれる臭気成分を低減も
しくは除去する脱臭触媒において、銀とマンガンの元素
またはその化合物を含む活性成分を、全細孔容積が0.
20cm^3/g以上で半径1,000Åから30,0
00Åの範囲の細孔の容積の合計量が全細孔容積の80
vol%以上である細孔分布を有するコーディェライト
、ムライト、アルミナ等からなる多孔質材料に担持する
ことを特徴とする脱臭用触媒。(1) Active ingredients containing silver and manganese elements or their compounds in deodorizing catalysts that reduce or remove odor components contained in smoke and exhaust gas generated from heating equipment such as food cookers, garbage incinerators, and painting equipment. , the total pore volume is 0.
20cm^3/g or more, radius 1,000Å to 30,0
The total volume of pores in the range of 00 Å is 80 Å of the total pore volume.
A deodorizing catalyst characterized in that it is supported on a porous material made of cordierite, mullite, alumina, etc. having a pore distribution of vol% or more.
とを特徴とする加熱装置。(2) A heating device characterized in that the deodorizing catalyst according to claim 1 is disposed in an exhaust section.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2232722A JPH04114744A (en) | 1990-09-03 | 1990-09-03 | Deodorizing catalyst and heating apparatus using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2232722A JPH04114744A (en) | 1990-09-03 | 1990-09-03 | Deodorizing catalyst and heating apparatus using the same |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04114744A true JPH04114744A (en) | 1992-04-15 |
Family
ID=16943763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2232722A Pending JPH04114744A (en) | 1990-09-03 | 1990-09-03 | Deodorizing catalyst and heating apparatus using the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04114744A (en) |
-
1990
- 1990-09-03 JP JP2232722A patent/JPH04114744A/en active Pending
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